选择性离子交换法脱除水中NH3-N

采用储量较大的黑龙江省嫩江天然斜发沸石,对其脱除NH_3-N的能力、预处理及洗脱再生方法、交换平衡、交换动力学等进行系统的研究,并对沸石床层的交换过程进行数学模型计算。     

海洋巨藻生物吸附剂对Hg~(2 )吸附性能的研究

就丰产廉价的海洋巨藻(Durvillaea Potatorum)所制的生物吸附剂对Hg2 的吸附性能进行了研究,该生物吸附剂经特殊的稳定化预处理而得。研究表明,该生物吸附剂的Hg2 吸附容量对溶液的pH值十分敏感,在pH=3时,最大吸附容量达到3.1mmol/g(干重),在溶液pH=0.4～5.0的范围内,Hg2 的吸附容量为0.49—3.1mmol/g(干重);溶液中的C1-能显著地降低生物吸附剂对Hg2 的吸附容量;其对Hg2 的去除率可达到99％以上。该生物吸附剂可以有效地去除工业废水中的Hg2 。     

水葫芦对Zn2+、Cd2+和Fe3+的去除速率

通过静态水培实验和原子吸收分光光度法的测定,发现水葫芦对个别重金属离子累积去除率头两天为Zn≈Cd>Fe,以后为Fe>Zn>Cd;5天中,Cd2 在水葫芦老黄茎叶中的积累量增长了130 0倍;在混合离子培养液中,Zn2 的去除速率明显下降,而Cd2 和Fe3 变化不明显。表明水葫芦在治理含镉废水方面有良好的应用前景。     

沸石在水处理中的应用

本文介绍了中国沸石的种类及其分布概况，以产自甘肃省白银市的斜发沸石为研究对象，对其化学组成及分子晶格形式作了较为详尽的阐述，经实验室检测出其化学组成及物化指标，且对沸石作为吸附剂、离子交换剂、催化剂处理废水的作用机理进行了深入的探讨，对于天然沸石改性进行了实验研究，得出采用氯化钠溶液对天然沸石改性的效果比较理想，改性溶液的最佳浓度为0．9mol/L。研究沸石在沸水处理领域中的应用，分析了沸石处理各类废水的机理，并对沸石处理废水的前景进行了展望。     

离聚物（MPET）对水中铬离子的吸附性能研究

研究了离聚物（MPET）粉末对Cr^3 的吸附性能，探讨了不同的吸附温度、时间、pH值和不同的初始浓度对吸附性能的影响，实验发现Cr^3 在较低温度下和pH为4时能被MPETO分末很好地吸附，最大饱和吸附量为11.80mg/g，实验表明MPET废纤维很可能发展成为一种经济的吸附重金属离子的材料。     

3,5-二甲基吡唑磷酸盐硝化抑制作用初探

采用室内培养实验的方法,以不加抑制剂的尿素作为对照,对比研究DMPP及它的同分异构体3,5-二甲基吡唑磷酸盐作为硝化抑制剂对尿素氮在土壤中转化的影响.结果表明,3,5-二甲基吡唑磷酸盐具有一定的硝化抑制作用.在培养期间,施加3,5-二甲基吡唑磷酸盐的土壤中硝态氮的含量一周后始终低于对照,铵态氮的含量一用后始终高于对照.但在培养试验中后期(三周以后),3,5-二甲基吡唑磷酸盐的硝化抑制效果劣于DMPP.3,5-二甲基吡唑磷酸盐能否作为新型硝化抑制剂,还要对它的生理、生态效应等进行进一步的研究.     

改性稻草吸附铜离子的动力学机理

研究表明稻草改性后吸附铜离子的能力得到很大提高。研究表明吸附相当好地符合假二级吸附速率模型,测定了在4个温度下(15℃,27℃,37℃,50℃)的吸附速率常数。吸附平衡可用Langmiur吸附模型和Freundlich吸附模型处理。讨论了pH对吸附的影响。     

Insights into the mechanism of the deterioration of mainstream partial nitritation/anammox under low residual ammonium

Residual ammonium is a critical parameter affecting the stability of mainstream partial nitritation/anammox (PN/A), but the underlying mechanism remains unclear. In this study, mainstream PN/A was established and operated with progressively decreasing residual ammonium. PN/A deteriorated as the residual ammonium decreased to below 5 mg/L, and this was paralleled by a significant loss in anammox activity in situ and an increasing nitrite oxidation rate. Further analysis revealed that the low-ammonium condition directly decreased anammox activity in situ via two distinct mechanisms. First, anammox bacteria were located in the inner layer of the granular sludge, and thus were disadvantageous when competing for ammonium with ammonium-oxidizing bacteria (AOB) in the outer layer. Second, the complete ammonia oxidizer (comammox) was enriched at low residual ammonium concentrations because of its high ammonium affinity. Both AOB and comammox presented kinetic advantages over anammox bacteria. At high residual ammonium concentrations, nitrite-oxidizing bacteria (NOB) were effectively suppressed, even when their maximum activity was high due to competition for nitrite with anammox bacteria. At low residual ammonium concentrations, the decrease in anammox activity in situ led to an increase in nitrite availability for nitrite oxidation, facilitating the activation of NOB despite the dissolved oxygen limitation (0.15–0.35 mg/L) for NOB persisting throughout the operation. Therefore, the deterioration of mainstream PN/A at low residual ammonium was primarily triggered by a decline in anammox activity in situ. This study provides novel insights into the optimized design of mainstream PN/As in engineering applications.     

预处理的铜绿假单胞菌对Cu2+的生物吸附研究

从电镀废水污泥中分离，纯化获一高抗铜菌株，经鉴定为铜绿假单胞菌（Pseudomonas aeruginosa)，采用不同浓度盐酸对铜绿假单胞菌进行预处理，同时考察了不同因素如溶液的pH，温度，摇床转速，接触反应时间对未处理菌和预处理的影响，结果表明，经0．1NHCl预处理的菌体具有最佳吸附效果，pH、摇床转速对菌体的吸附具有较显著影响，温度对菌体吸附影响不大。     

Enhanced removal of high-As(Ⅲ) from Cl(-Ⅰ)-diluted SO4(-Ⅱ)-rich wastewater at pH 2.3 via mixed tooeleite and(Cl(-Ⅰ)-free) ferric arsenite hydroxychloride formation

An advanced cost-saving method of removal of high-As(Ⅲ) from SO₄(-Ⅱ)-rich metallurgi cal wastewater has been developed by diluting the SO₄(-Ⅱ) content with As(Ⅲ)-Cl(-Ⅰ)-rich metallurgical wastewater and then by the direct precipitation of As(Ⅲ) with Fe(Ⅲ) at pH2.3.As(Ⅲ) removal at various SO₄(-Ⅱ)/Cl(-Ⅰ) molar ratios and temperatures was investigated The results showed that 65.2–98.2%of As(III) immobilization into solids occurred at the SO₄(Ⅱ)/Cl(-Ⅰ) mo...